Canonical Allele Identifier: CA432536347
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1123711
ClinVar RCV Id: RCV001454854
dbSNP Id: rs773519476
gnomAD v4: 3-10141982-G-C
MyVariant Identifiers: chr3:g.10183666G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141982G>C , CM000665.2:g.10141982G>C GRCh38
NC_000003.11:g.10183666G>C , CM000665.1:g.10183666G>C GRCh37
NC_000003.10:g.10158666G>C NCBI36
NG_008212.3:g.5348G>C , LRG_322:g.5348G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.135G>C ENSP00000512434.1:p.Pro45=
ENST00000696143.1:c.135G>C ENSP00000512435.1:p.Pro45=
ENST00000696153.1:c.135G>C ENSP00000512444.1:p.Pro45=
ENST00000256474.3:c.135G>C MANE Select ENSP00000256474.3:p.Pro45=
ENST00000256474.2:c.135G>C ENSP00000256474.2:p.Pro45=
ENST00000345392.2:c.135G>C ENSP00000344757.2:p.Pro45=
NM_000551.3:c.135G>C , LRG_322t1:c.135G>C NP_000542.1:p.Pro45=
NM_198156.2:c.135G>C NP_937799.1:p.Pro45=
XM_011534078.1:c.135G>C XP_011532380.1:p.Pro45=
NM_001354723.1:c.135G>C NP_001341652.1:p.Pro45=
NM_000551.4:c.135G>C MANE Select NP_000542.1:p.Pro45=
NM_001354723.2:c.135G>C NP_001341652.1:p.Pro45=
NM_198156.3:c.135G>C NP_937799.1:p.Pro45=